|
NM_004006.3:c.2636G>A
MANE Select
|
NP_003997.2:p.Arg879Gln
|
|
ENST00000357033.9:c.2636G>A
MANE Select
|
ENSP00000354923.3:p.Arg879Gln
|
|
NM_000109.3:c.2612G>A
|
NP_000100.2:p.Arg871Gln
|
|
NM_000109.4:c.2612G>A
|
NP_000100.3:p.Arg871Gln
|
|
NM_004006.2:c.2636G>A , LRG_199t1:c.2636G>A
|
NP_003997.1:p.Arg879Gln
|
|
NM_004009.3:c.2624G>A
|
NP_004000.1:p.Arg875Gln
|
|
NM_004010.3:c.2267G>A
|
NP_004001.1:p.Arg756Gln
|
|
ENST00000357033.8:c.2636G>A
|
ENSP00000354923.3:p.Arg879Gln
|
|
ENST00000378677.6:c.2624G>A
|
ENSP00000367948.2:p.Arg875Gln
|
|
ENST00000420596.5:c.94-119887G>A
|
ENSP00000399897.1:n.94-119887G>A
|
|
ENST00000448370.5:c.94-120376G>A
|
ENSP00000388559.1:n.94-120376G>A
|
|
ENST00000488902.5:n.336-268023G>A
|
|
|
ENST00000619831.4:c.2624G>A
|
ENSP00000479270.1:p.Arg875Gln
|
|
ENST00000620040.4:c.2636G>A
|
ENSP00000478150.1:p.Arg879Gln
|
|
ENST00000682899.1:n.2843G>A
|
|
|
ENST00000683985.1:n.2843G>A
|
|
|
XM_006724468.2:c.2636G>A
|
XP_006724531.1:p.Arg879Gln
|
|
XM_006724469.2:c.2612G>A
|
XP_006724532.1:p.Arg871Gln
|
|
XM_006724469.3:c.2612G>A
|
XP_006724532.1:p.Arg871Gln
|
|
XM_006724470.2:c.2636G>A
|
XP_006724533.1:p.Arg879Gln
|
|
XM_006724470.3:c.2636G>A
|
XP_006724533.1:p.Arg879Gln
|
|
XM_006724471.2:c.2636G>A
|
XP_006724534.1:p.Arg879Gln
|
|
XM_006724472.2:c.2507G>A
|
XP_006724535.1:p.Arg836Gln
|
|
XM_006724473.2:c.2636G>A
|
XP_006724536.1:p.Arg879Gln
|
|
XM_006724474.2:c.2636G>A
|
XP_006724537.1:p.Arg879Gln
|
|
XM_006724474.3:c.2636G>A
|
XP_006724537.1:p.Arg879Gln
|
|
XM_006724475.2:c.2636G>A
|
XP_006724538.1:p.Arg879Gln
|
|
XM_011545467.1:c.2636G>A
|
XP_011543769.1:p.Arg879Gln
|
|
XM_011545468.1:c.2636G>A
|
XP_011543770.1:p.Arg879Gln
|
|
XM_011545468.2:c.2636G>A
|
XP_011543770.1:p.Arg879Gln
|
|
XM_011545469.1:c.2636G>A
|
XP_011543771.1:p.Arg879Gln
|
|
XM_017029328.1:c.2636G>A
|
XP_016884817.1:p.Arg879Gln
|
|
XM_017029329.1:c.2636G>A
|
XP_016884818.1:p.Arg879Gln
|
|
XM_017029330.2:c.2636G>A
|
XP_016884819.1:p.Arg879Gln
|
